ENST00000278853.10:c.858C>T
MANE Select
|
ENSP00000278853.5:p.Phe286=
|
|
ENST00000278853.9:c.858C>T
|
ENSP00000278853.5:p.Phe286=
|
|
ENST00000537203.5:n.477C>T
|
|
|
ENST00000540908.1:c.286C>T
|
|
|
ENST00000542971.1:n.148C>T
|
|
|
ENST00000620319.1:c.-22C>T
|
ENSP00000480463.1:n.-22C>T
|
|
NM_207341.3:c.858C>T
|
NP_997224.2:p.Phe286=
|
|
XM_011544852.1:c.-22C>T
|
XP_011543154.1:n.-22C>T
|
|
XM_011544853.1:c.-22C>T
|
XP_011543155.1:n.-22C>T
|
|
XM_011544852.2:c.-22C>T
|
XP_011543154.1:n.-22C>T
|
|
XM_011544853.2:c.-22C>T
|
XP_011543155.1:n.-22C>T
|
|
NM_001391943.1:c.-22C>T
|
NP_001378872.1:n.-22C>T
|
|
NM_001391944.1:c.-333C>T
|
NP_001378873.1:n.-333C>T
|
|
NM_207341.4:c.858C>T
MANE Select
|
NP_997224.2:p.Phe286=
|
|